Abstract
The nuclear exosome is involved in a large number of RNA processing and surveillance pathways. RNase III cleavage intermediates destined to be 3'-processed or degraded can be detected when the Rrp6p subunit of the nuclear exosome is absent. Here we show that these processing and degradation intermediates are polyadenylated, and that their polyadenylation is dependent on the activity of Trf4p and Trf5p, two variant poly(A) polymerases. Polyadenylation of cleavage intermediates was inhibited when Trf4p was absent, and reduced to various extents in the absence of Trf5p, suggesting that these two poly(A) polymerases play functionally distinct roles in the polyadenylation of these RNA species. Finally, in the absence of Trf4p, we observed 3'-extended forms of the U4 snRNA that are similar to those observed in the absence of Rrp6p. These results suggest that polyadenylation of RNA processing intermediates plays a functional role in RNA processing pathways and is not limited to RNA surveillance functions.
MeSH Terms
Animals
Cell Nucleus/metabolism
DNA-Directed DNA Polymerase/metabolism
DNA-Directed RNA Polymerases/metabolism
Exonucleases/metabolism
Polyadenylation
RNA 3' End Processing
RNA, Messenger/metabolism
RNA, Small Nuclear/metabolism
RNA, Small Nucleolar/metabolism
Ribonuclease III/metabolism
Saccharomyces cerevisiae Proteins/metabolism
Chemicals
RNA, Messenger
RNA, Small Nuclear
RNA, Small Nucleolar
Saccharomyces cerevisiae Proteins
DNA-Directed RNA Polymerases
Trf5 protein, S cerevisiae
DNA-Directed DNA Polymerase
PAP2 protein, S cerevisiae
Exonucleases
RNT1 protein, S cerevisiae
Ribonuclease III
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Egecioglu Defne E
Department of Chemistry and Biochemistry and the Molecular Biology Institute, University of California Los Angeles, Box 951569, Los Angeles, CA 90095-1569, USA.
Henras Anthony K
Chanfreau Guillaume F
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